6242 - Upstream Principal Cqv Engineer / Lead Validation Engineer

Veristainc

Holly Springs, NC, United States
On-site
Upstream bioprocessing systems
Commissioning, qualification, and validation (cqv)
Cgmp and regulatory expectations
Verista is seeking an Upstream Principal CQV Engineer to support commissioning, qualification, and validation activities in biopharmaceutical manufacturing. The ideal candidate should have hands-on experience in upstream bioprocessing systems and a strong understanding of the CQV lifecycle

Job Summary

  • Support commissioning, qualification, and validation (CQV) activities for upstream bioprocess equipment and systems.
  • Author, review, and execute CQV lifecycle documentation including commissioning test protocols, IQ, OQ, PQ, and validation summary reports.
  • Provide technical support for upstream bioprocess unit operations, including bioreactors, media and buffer preparation systems, and cell culture support equipment.

Matching Summary

Match Score: 85

Verista is seeking an Upstream Principal CQV Engineer to support commissioning, qualification, and validation activities in biopharmaceutical manufacturing. The ideal candidate should have hands-on experience in upstream bioprocessing systems and a strong understanding of the CQV lifecycle.

Skills & Requirements

Must-have

  • Upstream bioprocessing systems
  • Commissioning, Qualification, and Validation (CQV)
  • cGMP and regulatory expectations
  • Upstream unit operations and process equipment
  • Digital validation platforms

Nice-to-have

  • Empower growth and innovation
  • Team environment
  • Client success
  • Inclusive environment
  • Acquire new skills

Key Requirements

  • Hands-on experience in upstream bioprocessing systems
  • Experience with the CQV lifecycle
  • Experience with digital validation platforms such as Kneat
  • Ability to work independently while collaborating cross-functionally

Work Rights

Not specified

Tailored Resume

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